These are simple e-mail formats that you fill out and they respond back with LLMD,s located closest to you.
You must research each LLMD. To do this google for patient reviews or connect with your local Lyme support groups. Support groups offer first-hand experiences with LLMD’s in your area. Here are support groups near you;
Many LLMD’s don’t participate with insurances so your 1st appointment will be the most expensive. Be prepared. Bring ALL things Medical, ie, results of all blood work, medical procedures, medical providers, current symptoms, diagnosis’s.
Be sure to utilize Lymenet’s ‘search’ function located in the middle of the home page. It contains valuable information from Lymenet’s members journey’s with ALL Lyme related feed-back and progresses. It can answer many many of your questions!
I will send you a private message. Healing Wishes.
Posts: 2977 | From Florida | Registered: Nov 2016
| IP: Logged |
I know you are new to Lymenet, but you should add "in CA" to the title of your post so people will know specifically where you are looking. To do this click the pencil/paper tab, make your changes, then click "Edit Post".
Contact the CA Lyme Support Groups - they would know better about CA.
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/